Label: BETADINE SURGICAL SCRUB- povidone-iodine solution
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NDC Code(s):
67618-151-01,
67618-151-04,
67618-151-16,
67618-151-17, view more67618-151-32
- Packager: Atlantis Consumer Healthcare, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 22, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
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DOSAGE & ADMINISTRATION
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Surgical hand scrub:
- wet hands with water
- spread about 5 cc (1 teaspoonful) of Scrub over both handsand forearms
- without adding more water, scrub thoroughly for 2 1/2 to3 minutes
- use a sponge if desired. Clean thoroughly under fingernails.
- add a little water and develop copious suds. Rinse thoroughlyunder running water.
- repeat the entire procedure using another 5 cc of Scrub
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Antiseptic hand wash:
- wet hands with water and pour about 5 cc of Scrub on hands
- rub hands vigorously together for at least 15 seconds, coveringall surfaces
- rinse and dry with a disposable towel
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Surgical hand scrub:
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BETADINE SURGICAL SCRUB
povidone-iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67618-151 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE .075 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0) NONOXYNOL-9 (UNII: 48Q180SH9T) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67618-151-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/1996 2 NDC:67618-151-16 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/1996 01/31/2025 3 NDC:67618-151-17 1 in 1 CARTON 07/01/1996 01/31/2025 3 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:67618-151-32 946 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/1996 11/30/2024 5 NDC:67618-151-01 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/1996 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 07/01/1996 Labeler - Atlantis Consumer Healthcare, Inc. (118983925) Registrant - Atlantis Consumer Healthcare, Inc. (118983925)